Canonical Allele Identifier: CA2317700568
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401557G= , CM000681.2:g.1401557G= GRCh38
NC_000019.9:g.1401556G= , CM000681.1:g.1401556G= GRCh37
NC_000019.8:g.1352556G= NCBI36
NG_009785.1:g.4997C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447102.8:c.-81C= ENSP00000403536.2:n.-81C=
ENST00000447102.7:c.-81C= ENSP00000403536.2:n.-81C=
NM_000156.5:c.-81C= NP_000147.1:n.-81C=
NM_138924.2:c.-81C= NP_620279.1:n.-81C=